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DESCRIBE <http://purl.uniprot.org/SHA-384/310E7E9F0B26B2D19C9FCCFDCD4D362B90EA3AAF45AD27189387F1CD258BB411475C72EAA68C91DDB0C021E6B130FDA0>
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http://purl.uniprot.org/SHA-384/310E7E9F0B26B2D19C9FCCFDCD4D362B90EA3AAF45AD27189387F1CD258BB411475C72EAA68C91DDB0C021E6B130FDA0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/310E7E9F0B26B2D19C9FCCFDCD4D362B90EA3AAF45AD27189387F1CD258BB411475C72EAA68C91DDB0C021E6B130FDA0
http://www.w3.org/2000/01/rdf-schema#comment
"Results indicate that SYNGAP1 disruption is a cause of autosomal dominant nonsyndromic mental retardation; Observational study of gene-disease association. (HuGE Navigator)"
xsd:string
http://purl.uniprot.org/uniprot/#_BBF00AC308CB75F40FBF57734A048F5856101FB3F0A4FF35DB55D415A333FE0A0B45B73C552EB171A33102FC15CBC134
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/310E7E9F0B26B2D19C9FCCFDCD4D362B90EA3AAF45AD27189387F1CD258BB411475C72EAA68C91DDB0C021E6B130FDA0
http://purl.uniprot.org/uniprot/B7ZCA0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/310E7E9F0B26B2D19C9FCCFDCD4D362B90EA3AAF45AD27189387F1CD258BB411475C72EAA68C91DDB0C021E6B130FDA0
http://purl.uniprot.org/uniprot/#_B7ZCA0-mappedCitation-19196676
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/310E7E9F0B26B2D19C9FCCFDCD4D362B90EA3AAF45AD27189387F1CD258BB411475C72EAA68C91DDB0C021E6B130FDA0